Home / Brand archive
5 reported ongoing
5 records in this archive. Latest source date Feb 24, 2023.
FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
Non-Sterility: FDA analysis found unopened tubes to be contaminated with bacteria.
Class IReported ongoing
Distribution: Product was imported by one distributor, Delsam Pharma, LLC, who further distributed the product via internet sales Nationwide in the USA.
Non-Sterility: FDA analysis found unopened products to have bacterial contamination.
Class IReported ongoing
Distribution: Product was distributed to two distributors who further distributed Nationwide in the USA.
CGMP Deviations: All other lots of eye drops are being recalled due to CGMP Deviations because they were manufactured in the same facility under the same conditions as the lots found to be contaminated.
Class IIReported ongoing
Distribution: Product was distributed to two distributors who further distributed Nationwide in the USA.
Non-Sterility: FDA analysis found unopened products to have bacterial contamination.
Class IReported ongoing
Distribution: Product was distributed to two distributors who further distributed Nationwide in the USA.
CGMP Deviations: All other lots of eye drops are being recalled due to CGMP Deviations because they were manufactured in the same facility under the same conditions as the lots found to be contaminated.
Class IIReported ongoing
Distribution: Product was distributed to two distributors who further distributed Nationwide in the USA.
These examples come from this result page and are not a ranking of every recall reason.
This archive contains 5 records, including 5 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.
Compare the product, firm and lot, date, model or serial identifiers with the notice. Use the label-check guide if you need help locating an identifier.
A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.
This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. Check source coverage and the agency's current notices.
Use monthly archives or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.